rs587778944

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	0	common in clinvar
(-;A)	6	Lynch syndrome, pathogenic mutation

Make rs587778944(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

36996677

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs587778944
dbSNP (classic)	rs587778944
ClinGen	rs587778944
ebi	rs587778944
HLI	rs587778944
Exac	rs587778944
Gnomad	rs587778944
Varsome	rs587778944
LitVar	rs587778944
Map	rs587778944
PheGenI	rs587778944
Biobank	rs587778944
1000 genomes	rs587778944
hgdp	rs587778944
ensembl	rs587778944
geneview	rs587778944
scholar	rs587778944
google	rs587778944
pharmgkb	rs587778944
gwascentral	rs587778944
openSNP	rs587778944
23andMe	rs587778944
SNPshot	rs587778944
SNPdbe	rs587778944
MSV3d	rs587778944
GWAS Ctlg	rs587778944

Max Magnitude

6

ClinVar
Risk	rs587778944(A;A)
Alt	rs587778944(A;A)
Reference	Rs587778944(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37038168dupA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075356.2,